Brain & Nervous System More Neurological Diseases Myasthenia Gravis Guide Myasthenia Gravis Guide Overview Symptoms Causes Diagnosis Treatment Coping Causes and Risk Factors of Myasthenia Gravis By Sherry Christiansen Sherry Christiansen Sherry Christiansen is a medical writer with a healthcare background. She has worked in the hospital setting and collaborated on Alzheimer's research. Learn about our editorial process Updated on March 05, 2021 Medically reviewed by David Ozeri, MD Medically reviewed by David Ozeri, MD LinkedIn David Ozeri, MD, is a board-certified rheumatologist. He is based in Tel Aviv, Israel, where he does research at Sheba Medical Center. Previously, he practiced at New York-Presbyterian Hospital. Learn about our Medical Expert Board Print Table of Contents View All Table of Contents Common Causes Genetics Cardiovascular Involvement Lifestyle Risk Factors Next in Myasthenia Gravis Guide How Myasthenia Gravis Is Diagnosed The cause of myasthenia gravis (MG) is an autoimmune reaction in which the body’s immune system mistakenly attacks specific proteins in the muscles, causing weakness. A genetic predisposition to autoimmune disorders and certain lifestyle factors contribute to the risk of this disease. There is no cure for MG, but some treatments can help alleviate its symptoms. Although myasthenia gravis can be diagnosed at any age, including during childhood, it is most often seen in women less than 40 and men more than 60. This article explores the common causes and risk factors associated with myasthenia gravis. Jose Luis Pelaez / Getty Images Common Causes When a person has MG, antibodies—called acetylcholine receptor (AChR) antibodies—misguidedly attack the receptors for acetylcholine, a chemical messenger released by nerve cells to stimulate muscle contractions. As a result of the interference with the transmission of nerve-to-muscle signaling, muscle weakness develops. A person with MG can also have antibodies—called muscle-specific receptor tyrosine kinase (MuSK) antibodies—produced against proteins located on the surface of the muscle membrane. Causes of Immunodeficiency The specific underlying cause of the abnormal immune response, which occurs in people with MG, is not well known. However, studies have discovered a link between people with MG and abnormalities in the form of enlargement of the thymus gland. According to Harvard Health, nearly 80% of people with MG have distinct abnormalities of the thymus gland. Causes of Ocular Myasthenia Gravis Ocular MG is a type of MG that involves the muscles that move the eyes and eyelids. This causes: Double visionDifficulty focusing the eyesDrooping eyelids Verywell / Alexandra Gordon Nearly 15% of people with MG only have ocular MG gravis. Over time, if weakness develops in other muscles in the body, the type of myasthenia gravis may change from ocular myasthenia gravis to generalized myasthenia gravis. Causes of Transient Neonatal Myasthenia Gravis Some newborns (with mothers who have MG) develop muscle weakness temporarily. This is a condition called transient neonatal MG. The cause of transient neonatal myasthenia gravis is antiacetylcholine receptor antibodies that travel through the placenta to the unborn child during pregnancy. It takes about two months for the mother’s antibodies to be cleared from the baby’s system, resulting in the subsiding of muscle weakness in the baby. Genetics Most cases of MG do not involve a family history of the disease; MG is thought to occur sporadically for unknown reasons. But that is not always the case. In 5% of those with myasthenia gravis, there is a family member with some type of autoimmune disorder. Also, genetics are thought to possibly play a role in predisposing a person to MG. This is because specific antigens—called human leukocyte antigens—which are genetically determined, are thought to affect a person’s risk of getting certain types of diseases. Commonly, people with MG develop other types of autoimmune disease, including thyroid disorders and systemic (involving the entire body) lupus erythematosus. Individuals with MG also have an increased frequency of certain genetically determined human leukocyte antigens (HLAs), suggesting that genetic predisposition may play some role in the development of myasthenia gravis. Genetic Predisposition for Autoimmune Diseases Unlike many other types of disorders, MG is not considered a disease that is directly inherited, but rather, there may be a genetic predisposition for autoimmune diseases. Cardiovascular Involvement In addition to its impact on the neuromuscular system, MG impacts other organs and systems of the body, The disease is known to cause a high prevalence of heart problems in 10% to 15% of those with MG who also have thymoma. Cardiovascular involvement may include: Cardiomyopathy (enlargement of the heart) Heart failure Cardiac arrhythmias (a rhythm disorder of the heart rate) Coronary valvular disease According to a 2014 study, the heart muscle is a target for autoimmune inflammation in MG. In addition to thymoma posing a risk factor to heart muscle involvement in those with MG, other factors may influence this risk as well, including: Advancing ageThe presence of anti-Kv1 antibodies Lifestyle Risk Factors A 2018 Swedish study found that those with late-onset disease had a more disadvantageous pattern of lifestyle-related risk factors, and a higher rate of: SmokingObesityPhysical inactivityInsufficient diet (including a lower rate of fish consumption) General Risk Factors General risk factors found to increase the chance of a person getting MG include: Being a woman between the ages of 20 to 30Being a man between the ages of 60 to 70Having specific genetic markers called HLA-B8 or DR3Neonates (newborn infants) with mothers who have abnormal antibodies that have entered the baby’s body via the placenta during pregnancy Prevention Measures Although the causes of MG are unknown and cannot be changed, flare-ups may be controlled by implementing some lifestyle changes. If you have been diagnosed with MG, many lifestyle changes may help prevent flare-ups and lower the chances of worsening symptoms, these lifestyle changes include: Getting plenty of sleepTaking rest periods when neededAvoiding strenuous or exhausting activitiesStaying out of the extreme heat and coldCoping with emotional stressorsAvoiding infections when possibleWorking with your healthcare provider to avoid drugs that worsen MG A Word From Verywell At Verywell Health, we know that being diagnosed with a condition such as MG is no small undertaking. The condition is lifelong, but early diagnosis and intervention are the keys to effectively managing the disease on a long-term basis. If you suspect you may have myasthenia gravis, it’s important to call your healthcare provider right away. 9 Sources Verywell Health uses only high-quality sources, including peer-reviewed studies, to support the facts within our articles. Read our editorial process to learn more about how we fact-check and keep our content accurate, reliable, and trustworthy. National Institute of Neurological Disorders and Stroke. Myasthenia gravis fact sheet. Harvard Health. Myasthenia gravis. Myasthenia Gravis Foundation of America. Learn more about MG. University of Maryland St. Joseph Medical Center. Neuromuscular - myasthenia gravis. National Organization for Rare Disorders. Myasthenia gravis. Genetic and Rare Diseases Information Center. Myasthenia gravis. Shivamurthy P, Parker MW. Cardiac manifestations of myasthenia gravis: A systematic review. IJC Metabolic & Endocrine. 2014;5:3-6. doi:10.1016/j.ijcme.2014.08.003 Suzuki S, Utsugisawa K, Nagane Y, Suzuki N. Three types of striational antibodies in myasthenia gravis. Autoimmune Diseases. 2011;2011:1-7. doi:10.4061/2011/740583 Westerberg, E. UPPSALA UNIERSITET. Environmental factors of importance in myasthenia gravis. By Sherry Christiansen Sherry Christiansen is a medical writer with a healthcare background. She has worked in the hospital setting and collaborated on Alzheimer's research. See Our Editorial Process Meet Our Medical Expert Board Share Feedback Was this page helpful? Thanks for your feedback! What is your feedback? Other Helpful Report an Error Submit